| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119702827-119703119 | Common:6; Rare:92 | ||||
| chr3:120093416-120093893 | Rare:135 | ||||
| chr3:120094287-120094801 | Common:5; Rare:162 | ||||
| chr3:120349296-120349447 | Common:2; Rare:51 | ||||
| chr3:120596060-120596448 | Common:3; Rare:139 | ||||
| chr3:120596752-120596782 | Rare:11 | ||||
| chr3:120742494-120742777 | Common:2; Rare:81 | ||||
| chr3:121545946-121546192 | Common:1; Rare:59 | ||||
| chr3:121660821-121661009 | Rare:38 | ||||
| chr3:121749119-121749298 | Rare:28 | ||||
| chr3:121749431-121749550 | Common:1; Rare:20 | ||||
| chr3:121749637-121750021 | Common:1; Rare:88 | ||||
| chr3:121834956-121835263 | Common:3; Rare:103; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383178-122383323 | Common:1; Rare:46 | ||||
| chr3:122384030-122384291 | Common:3; Rare:90 |